Effect of Sintering Temperature on Adhesion Property and Electrochemical Activity of Pt/YSZ Electrode

The (Pt/YSZ)/YSZ sensor unit is the basic component of the NO_x sensor, which can detect the emission of nitrogen oxides in exhaust fumes and optimize the fuel combustion process. In this work, the effect of sintering temperature on adhesion property and electrochemical activity of Pt/YSZ electrode was investigated. Pt/YSZ electrodes were prepared at different sintering temperatures. The microstructure of the Pt/YSZ electrodes, as well as the interface between Pt/YSZ electrode and YSZ electrolyte, were observed by SEM. Chronoamperometry, linear scan voltammetry, and AC impedance were tested by the electrochemical workstation. The results show that increasing the sintering temperature (≤1500 °C) helped to improve adhesion property and electrochemical activity of the Pt/YSZ electrode, which benefited from the formation of the porous structure of the Pt/YSZ electrode. For the (Pt/YSZ) electrode/YSZ electrolyte system, O²⁻ in YSZ is converted into chemisorbed O₂ on Pt/YSZ, which is desorbed into the gas phase in the form of molecular oxygen; this process could be the rate-controlling step of the anodic reaction. Increasing the sintering temperature (≤1500 °C) could reduce the reaction activation energy of the Pt/YSZ electrode. The activation energy reaches the minimum value (1.02 eV) when the sintering temperature is 1500 °C.     

Phase Evaluation,Mechanical Properties and Thermal Behavior of Hot-Pressed LC-YSZ Composites for TBC Applications

In this work, La₂Ce₂O₇-yttria-stabilized zirconia (LC-YSZ) composites with different weight fractions of YSZ (40–70 wt.%) were prepared by hot pressing at 1400 °C and investigated as a material for thermal barrier-coating (TBC) applications. For this purpose, the effect of YSZ addition on the phase composition, microstructure, mechanical performance and thermal behavior was studied. X-ray diffraction analysis showed that the LC-YSZ composites were mainly composed of a cubic ZrO₂ and La₂O₃-CeO₂-ZrO₂ solid solution with a pyrochlore structure, indicating that the reaction between LC and YSZ took place during hot pressing. Scanning electron microscopy revealed the high microstructural stability of the prepared composites, as the pore formation was significantly controlled and a high relative density (>97%) was obtained. The microstructure of LC-YSZ bulk samples was relatively fine-grained, with an average grain size below or very close to 1 µm. YSZ doping improved the Vickers hardness of the LC-YSZ composites; the highest hardness, with value of 12 ± 0.62 GPa, was achieved for the composite containing 70 wt.% of YSZ. The fracture toughness of LC-YSZ composites was in the range from 2.13 to 2.5 MPa·m^1/2. No statistically significant difference in heat capacity or thermal conductivity was found between the composites with different content of YSZ. The results showed that LC-YSZ composites have relatively low thermal conductivities from room temperature (1.5–1.8 W·m⁻¹·K⁻¹) up to 1000 °C (2.5–3.0 W·m⁻¹·K⁻¹). This indicates that the prepared LC-YSZ composite materials are promising candidates for TBC applications.     

Micron-Sized Monodisperse Particle LiNi0.6Co0.2Mn0.2O2 Derived by Oxalate Solvothermal Process Combined with Calcination as Cathode Material for Lithium-Ion Batteries

Ni-rich cathode LiNi_xCo_yMn_1-x-yO₂ (NCM, x ≥ 0.5) materials are promising cathodes for lithium-ion batteries due to their high energy density and low cost. However, several issues, such as their complex preparation and electrochemical instability have hindered their commercial application. Herein, a simple solvothermal method combined with calcination was employed to synthesize LiNi_0.6Co_0.2Mn_0.2O₂ with micron-sized monodisperse particles, and the influence of the sintering temperature on the structures, morphologies, and electrochemical properties was investigated. The material sintered at 800 °C formed micron-sized particles with monodisperse characteristics, and a well-order layered structure. When charged–discharged in the voltage range of 2.8–4.3 V, it delivered an initial discharge capacity of 175.5 mAh g⁻¹ with a Coulombic efficiency of 80.3% at 0.1 C, and a superior discharge capacity of 135.4 mAh g⁻¹ with a capacity retention of 84.4% after 100 cycles at 1 C. The reliable electrochemical performance is probably attributable to the micron-sized monodisperse particles, which ensured stable crystal structure and fewer side reactions. This work is expected to provide a facile approach to preparing monodisperse particles of different scales, and improve the performance of Ni-rich NCM or other cathode materials for lithium-ion batteries.     

Effect of Sr Deficiency on Electrical Conductivity of Yb-Doped Strontium Zirconate

The effect of Sr-deficiency on microstructure, phase composition and electrical conductivity of Sr_xZr_0.95Yb_0.05O_3-δ (x = 0.94–1.00) was investigated via X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy and impedance spectroscopy. The samples were synthesized by a chemical solution method and sintered at 1600 °C. According to X-ray diffraction data, the samples with x = 0.96–1.00 were single-phase oxides possessing an orthorhombic perovskite-type structure; while zirconia-based minor phases arouse at x = 0.94, which was confirmed by the electron microscopy. Sr stoichiometry was shown to influence the electrical conductivity. The highest total and bulk conductivities, 6–10⁻⁴ Scm⁻¹ and 3–10⁻³ Scm⁻¹, respectively, at 600 °C in humid air (pH₂O = 3.2 kPa), were observed for the x = 0.98 composition. In the temperature range of 300–600 °C, the conductivity of the samples with x = 0.96–1.00 increased with the increase in humidity, which indicates a significant contribution of protonic defects to the charge transport. Electrical conductivity of Sr_xZr_0.95Yb_0.05O_3-δ was discussed in terms of the defect formation model and the secondary phases precipitation.     

Boost the Crystal Installation and Magnetic Features of Cobalt Ferrite/M-Type Strontium Ferrite Nanocomposites Double Substituted by La3+ and Sm3+ Ions (2CoFe2O4/SrFe12−2xSmxLaxO19)

Spinel cobalt ferrite/hexagonal strontium hexaferrite (2CoFe₂O₄/SrFe_12−2xSm_xLa_xO₁₉; x = 0.2, 0.5, 1.0, 1.5) nanocomposites were fabricated using the tartaric acid precursor pathway, and the effects of La³⁺–Sm³⁺ double substitution on the formation, structure, and magnetic properties of CoFe₂O₄/SrFe_12−2xSm_xLa_xO₁₉ nanocomposite at different annealing temperatures were assayed through X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry. A pure 2CoFe₂O₄/SrFe₁₂O₁₉ nanocomposite was obtained from the tartrate precursor complex annealed at 1100 °C for 2 h. The substitution of Fe³⁺ ion by Sm³–⁺La³⁺ions promoted the formation of pure 2CoFe₂O₄/SrFe₁₂O₁₉ nanocomposite at 1100 °C. The positions and intensities of the strongest peaks of hexagonal ferrite changed after Sm³⁺–La³⁺ substitution at ≤1100 °C. In addition, samples with an Sm³⁺–La³⁺ ratio of ≥1.0 annealed at 1200 °C for 2 h showed diffraction peaks for lanthanum cobalt oxide (La₃Co₃O₈; dominant phase) and samarium ferrite (SmFeO₃). The crystallite size range at all constituent phases was in the nanocrystalline range, from 39.4 nm to 122.4 nm. The average crystallite size of SrFe₁₂O₁₉ phase increased with the number of Sm³⁺–La³⁺ substitutions, whereas that of CoFe₂O₄ phase decreased with an x of up to 0.5. La–Sm co-doped ion substitution increased the saturation magnetization (Ms) value and the subrogated ratio to 0.2, and the Ms value decreased with the increasing number of double substitutions. A high saturation magnetization value (Ms = 69.6 emu/g) was obtained using a La³⁺–Sm³⁺ co-doped ratio of 0.2 at 1200 for 2 h, and a high coercive force value (Hc = 1192.0 Oe) was acquired using the same ratio at 1000 °C.     

On the Sintering Behavior of Nb2O5 and Ta2O5 Mixed Oxide Powders

A mixed oxide system consisting of Nb₂O₅ and Ta₂O_5, was subjected to annealing in air/hydrogen up to 950 °C for 1–4 h to study its sintering behavior. The thermogravimetric–differential scanning calorimetry (TGA–DSC) thermograms indicated the formation of multiple endothermic peaks at temperatures higher than 925 °C. Subsequently, a 30% Ta₂O₅ and 70% Nb₂O₅ (mol%) pellet resulted in good sintering behavior at both 900 and 950 °C. The scanning electron microscope (SEM) images corroborated these observations with necking and particle coarsening. The sintered pellets contained a 20.4 and 20.8% mixed oxide (Nb₄Ta₂O₁₅) phase, along with Ta₂O₅ and Nb₂O₅, at both 900 and 950 °C, indicating the possibility of the formation of a solid solution phase. In situ high-temperature X-ray diffraction (XRD) scans also confirmed the formation of the ternary oxide phase at 6 and 19.8% at 890 and 950 °C, respectively. The Hume–Rothery rules could explain the good sintering behavior of the Ta₂O₅ and Nb₂O₅ mixed oxides. An oxide composition of 30% Ta₂O₅ and 70% Nb₂O₅ (mol%) and a sintering temperature of 950 °C appeared adequate for fabricating well-sintered oxide precursors for subsequent electrochemical polarization studies in fused salts.     

The Effect of Sintering Temperature on the Phase Composition,Microstructure, and Mechanical Properties of Yttria-Stabilized Zirconia

It is known that the yttria-stabilized zirconia (YSZ) material has superior thermal, mechanical, and electrical properties. This material is used for manufacturing products and components of air heaters, hydrogen reformers, cracking furnaces, fired heaters, etc. This work is aimed at searching for the optimal sintering mode of YSZ ceramics that provides a high crack growth resistance. Beam specimens of ZrO₂ ceramics doped with 6, 7, and 8 mol% Y₂O₃ (hereinafter: 6YSZ, 7YSZ, and 8YSZ) were prepared using a conventional sintering technique. Four sintering temperatures (1450 °C, 1500 °C, 1550 °C, and 1600 °C) were used for the 6YSZ series and two sintering temperatures (1550 °C and 1600 °C) were used for the 7YSZ and 8YSZ series. The series of sintered specimens were ground and polished to reach a good surface quality. Several mechanical tests of the materials were performed, namely, the microhardness test, fracture toughness test by the indentation method, and single-edge notch beam (SENB) test under three-point bending. Based on XRD analysis, the phase balance (percentages of tetragonal, cubic, and monoclinic ZrO₂ phases) of each composition was substantiated. The morphology of the fracture surfaces of specimens after both the fracture toughness tests was studied in relation to the mechanical behavior of the specimens and the microstructure of corresponding materials. SEM-EDX analysis was used for microstructural characterization. It was found that both the yttria percentage and sintering temperature affect the mechanical behavior of the ceramics. Optimal chemical composition and sintering temperature were determined for the studied series of ceramics. The maximum transformation toughening effect was revealed for ZrO₂-6 mol% Y₂O₃ ceramics during indentation. However, in the case of a SENB test, the maximum transformation toughening effect in the crack tip vicinity was found in ZrO₂-7 mol% Y₂O₃ ceramics. The conditions for obtaining YSZ ceramics with high fracture toughness are discussed.     

Structure and Dielectric Behavior of Yb2O3-MgO Co-Doped 0.92BaTiO3-0.08(Na0.5Bi0.5)TiO3 Ferroelectric Relaxor

Dielectric properties and structure of 0.015Yb₂O₃-xMgO doped 0.92BaTiO₃-0.08(Na_0.5Bi_0.5)TiO₃ ceramics with x = 0.0–0.025 have been investigated. As Yb₂O₃-MgO was added into the BT-NBT, the phase changes from tetragonal to pseudo-cubic, with the tetragonality c/a decreases from 1.011 to 1.008 and XRD peaks broadened. The combined study of XRD and TEM image revealed a formation of core–shell structure in grains with core of 400–600 nm and the shell of a thickness 60–200 nm. There is a slowly phase transition against temperature from the variable temperature Raman analysis. The ferroelectric relaxor peak of BT-NBT decreases from ~4000 to ~2000 and a new broad dielectric peak with an equivalent maximum (ε_r′~2300) appears in the temperature dependent dielectric constant curve (ε_r′-T), which produces a flat ε_r′-T curve. Sample 0.92BaTiO₃-0.08(Na_0.5Bi_0.5)TiO₃-0.015Yb₂O₃-0.005 MgO and 0.92BaTiO₃-0.08(Na_0.5Bi_0.5)TiO₃-0.015Yb₂O₃-0.01MgO give a ε_r′ variation within ±14% and ±10% in 20–165 °C. The core–shell microstructure should take account for the flattened ε_r′–T behavior of these samples.     

Solid-State-Activated Sintering of ZnAl2O4 Ceramics Containing Cu3Nb2O8 with Superior Dielectric and Thermal Properties

Low-temperature co-fired ceramics (LTCCs) are dielectric materials that can be co-fired with Ag or Cu; however, conventional LTCC materials are mostly poorly thermally conductive, which is problematic and requires improvement. We focused on ZnAl₂O₄ (gahnite) as a base material. With its high thermal conductivity (~59 W·m⁻¹·K⁻¹ reported for 0.83ZnAl₂O₄–0.17TiO₂), ZnAl₂O₄ is potentially more thermally conductive than Al₂O₃ (alumina); however, it sinters densely at a moderate temperature (~1500 °C). The addition of only 4 wt.% of Cu₃Nb₂O₈ significantly lowered the sintering temperature of ZnAl₂O₄ to 910 °C, which is lower than the melting point of silver (961 °C). The sample fired at 960 °C for 384 h exhibited a relative permittivity (ε_r) of 9.2, a quality factor by resonant frequency (Q × f) value of 105,000 GHz, and a temperature coefficient of the resonant frequency (τ_f) of −56 ppm·K⁻¹. The sample exhibited a thermal conductivity of 10.1 W·m⁻¹·K⁻¹, which exceeds that of conventional LTCCs (~2–7 W·m⁻¹·K⁻¹); hence, it is a superior LTCC candidate. In addition, a mixed powder of the Cu₃Nb₂O₈ additive and ZnAl₂O₄ has a melting temperature that is not significantly different from that (~970 °C) of the pristine Cu₃Nb₂O₈ additive. The sample appears to densify in the solid state through a solid-state-activated sintering mechanism.     

Improvement of La0.8Sr0.2MnO3−δ Cathode Material for Solid Oxide Fuel Cells by Addition of YFe0.5Co0.5O3

The high efficiency of solid oxide fuel cells with La_0.8Sr_0.2MnO_3−δ (LSM) cathodes working in the range of 800–1000 °C, rapidly decreases below 800 °C. The goal of this study is to improve the properties of LSM cathodes working in the range of 500–800 °C by the addition of YFe_0.5Co_0.5O₃ (YFC). Monophasic YFC is synthesized and sintered at 950 °C. Composite cathodes are prepared on Ce_0.8Sm_0.2O_1.9 electrolyte disks using pastes containing YFC and LSM powders mixed in 0:1, 1:19, and 1:1 weight ratios denoted LSM, LSM1, and LSM1, respectively. X-ray diffraction patterns of tested composites reveal the presence of pure perovskite phases in samples sintered at 950 °C and the presence of Sr₄Fe₄O₁₁, YMnO₃, and La_0.775Sr_0.225MnO_3.047 phases in samples sintered at 1100 °C. Electrochemical impedance spectroscopy reveals that polarization resistance increases from LSM1, by LSM, to LSM2. Differences in polarization resistance increase with decreasing operating temperatures because activation energy rises in the same order and equals to 1.33, 1.34, and 1.58 eV for LSM1, LSM, and LSM2, respectively. The lower polarization resistance of LSM1 electrodes is caused by the lower resistance associated with the charge transfer process.     

Comparative Study on the Thermal Performance of Cr-CrxOy and YSZ-CoNiCrAlY Coatings Exposed at 900 °C

Yttria stabilized zirconia (YSZ) thermal barrier coatings (TBCs) deposited on CoNiCrAlY oxidation protective bond coats are commonly required in temperature regimes up to 1200 °C (e.g., hot gas turbine regions) due to their superior thermal behavior and mechanical properties. For temperatures up to around 900 °C, oxidation protection can be alternatively provided by metallic-ceramic Cr-Cr_xO_y coatings. For the present research, Cr-Cr_xO_y atmospheric plasma sprayed (APS) and YSZ-CoNiCrAlY APS-high velocity oxy-fuel TBC coatings were deposited on a NiCr20Co18Ti substrate. The samples were isothermally heat treated at 900 °C for 10 h in an environmental atmosphere and subsequently isothermally oxidized at the same temperature for 1200 h. Investigations of the physical, chemical, and mechanical properties were performed on the as-sprayed, heat-treated, and oxidized samples. The oxidation behavior, microhardness, cohesion, and adhesion of the samples were correlated with the microstructural investigations and compared to the conventional TBC system. It could be shown that heat treating decreased the Cr-Cr_xO_y coatings crack susceptibility and led to the formation of a protective thermally grown Cr oxide layer. The experimental work on the YSZ-CoNiCrAlY system revealed that the phase composition of the bond coat has a direct influence on the oxidation protection of the coating system.     

Fundamental signatures of short- and long-range electron transfer for the blue copper protein azurin at Au/SAM junctions

The blue copper protein from Pseudomonas aeruginosa, azurin, immobilized at gold electrodes through hydrophobic interaction with alkanethiol self-assembled monolayers (SAMs) of the general type [-S - (CH₂)_n - CH₃] (n = 4, 10, and 15) was employed to gain detailed insight into the physical mechanisms of short- and long-range biomolecular electron transfer (ET). Fast scan cyclic voltammetry and a Marcus equation analysis were used to determine unimolecular standard rate constants and reorganization free energies for variable n, temperature (2–55 °C), and pressure (5–150 MPa) conditions. A novel global fitting procedure was found to account for the reduced ET rate constant over almost five orders of magnitude (covering different n, temperature, and pressure) and revealed that electron exchange is a direct ET process and not conformationally gated. All the ET data, addressing SAMs with thickness variable over ca. 12 Å, could be described by using a single reorganization energy (0.3 eV), however, the values for the enthalpies and volumes of activation were found to vary with n. These data and their comparison with theory show how to discriminate between the fundamental signatures of short- and long-range biomolecular ET that are theoretically anticipated for the adiabatic and nonadiabatic ET mechanisms, respectively.     

Preparation and Properties of (YCa)(TiMn)O3?δ Ceramics Interconnect of Solid Oxide Fuel Cells

(YCa)(TiMn)O_3–δ ceramics prepared using a reaction-sintering process were investigated. Without any calcination involved, the mixture of raw materials was pressed and sintered directly. Y₂Ti₂O₇ instead of YTiO₃ formed when a mixture of Y₂O₃ and TiO₂ with Y/Ti ratio 1/1 were sintered in air. Y₂Ti₂O₇, YTiO_2.085 and some unknown phases were detected in Y_0.6Ca_0.4Ti_0.6Mn_0.4O_3–δ. Monophasic Y_0.6Ca_0.4Ti_0.4Mn_0.6O_3–δ ceramics were obtained after 1400–1500 °C sintering. Dense Y_0.6Ca_0.4Ti_0.4Mn_0.6O_3–δ with a density 4.69 g/cm³ was observed after 1500 °C/4 h sintering. Log σ for Y_0.6Ca_0.4Ti_0.6Mn_0.4O_3–δ increased from –3.73 Scm^–1 at 350 °C to –2.14 Scm^–1 at 700 °C. Log σ for Y_0.6Ca_0.4Ti_0.4Mn_0.6O_3–δ increased from –2.1 Scm^–1 at 350 °C to –1.36 Scm^–1 at 700 °C. Increasing Mn content decreased activation energy E_a and increased electrical conductivity. Reaction-sintering process is proved to be a simple and effective method to obtain (YCa)(TiMn)O_3–δ ceramics for interconnects in solid oxide fuel cells.     

Impact of Li3BO3 Addition on Solid Electrode-Solid Electrolyte Interface in All-Solid-State Batteries

All-solid-state lithium-ion batteries raise the issue of high resistance at the interface between solid electrolyte and electrode materials that needs to be addressed. The article investigates the effect of a low-melting Li₃BO₃ additive introduced into LiCoO₂- and Li₄Ti₅O₁₂-based composite electrodes on the interface resistance with a Li₇La₃Zr₂O₁₂ solid electrolyte. According to DSC analysis, interaction in the studied mixtures with Li₃BO₃ begins at 768 and 725 °C for LiCoO₂ and Li₄Ti₅O₁₂, respectively. The resistance of half-cells with different contents of Li₃BO₃ additive after heating at 700 and 720 °C was studied by impedance spectroscopy in the temperature range of 25–340 °C. It was established that the introduction of 5 wt% Li₃BO₃ into LiCoO₂ and heat treatment at 720 °C led to the greatest decrease in the interface resistance from 260 to 40 Ω cm² at 300 °C in comparison with pure LiCoO₂. An SEM study demonstrated that the addition of the low-melting component to electrode mass gave better contact with ceramics. It was shown that an increase in the annealing temperature of unmodified cells with Li₄Ti₅O₁₂ led to a decrease in the interface resistance. It was found that the interface resistance between composite anodes and solid electrolyte had lower values compared to Li₄Ti₅O₁₂|Li₇La₃Zr₂O₁₂ half-cells. It was established that the resistance of cells with the Li₄Ti₅O₁₂/Li₃BO₃ composite anode annealed at 720 °C decreased from 97.2 (x = 0) to 7.0 kΩ cm² (x = 5 wt% Li₃BO₃) at 150 °C.     

Enhancement of Y5−xPrxSb3−yMy (M = Sn,Pb) Electrodes for Lithium- and Sodium-Ion Batteries by Structure Disordering and CNTs Additives

The maximally disordered (MD) phases with the general formula Y_5−xPr_xSb_3−yM_y (M = Sn, Pb) are formed with partial substitution of Y by Pr and Sb by Sn or Pb in the binary Y₅Sb₃ compound. During the electrochemical lithiation and sodiation, the formation of Y_5-xPr_xSb_3-yM_yLi_z and Y_5−xPr_xSb_3−yM_yNa_z maximally disordered–high entropy intermetallic phases (MD-HEIP), as the result of insertion of Li/Na into octahedral voids, were observed. Carbon nanotubes (CNT) are an effective additive to improve the cycle stability of the Y_5−xPr_xSb_3−yM_y (M = Sn, Pb) anodes for lithium-ion (LIBs) and sodium-ion batteries (SIBs). Modification of Y_5−xPr_xSb_3−ySn_y alloys by carbon nanotubes allowed us to significantly increase the discharge capacity of both types of batteries, which reaches 280 mAh · g⁻¹ (for LIBs) and 160 mAh · g⁻¹ (for SIBs), respectively. For Y_5−xPrxSb_3−yPb_y alloys in which antimony is replaced by lead, these capacities are slightly smaller and are 270 mAh · g⁻¹ (for LIBs) and 155 mAh · g⁻¹ (for SIBs), respectively. Results show that structure disordering and CNT additives could increase the electrode capacities up to 30% for LIBs and up to 25% for SIBs.     

Triple Perovskite Nd1.5Ba1.5CoFeMnO9−δ-Sm0.2Ce0.8O1.9 Composite as Cathodes for the Intermediate Temperature Solid Oxide Fuel Cells

Triple perovskite has been recently developed for the intermediate temperature solid oxide fuel cell (IT-SOFC). The performance of Nd_1.5Ba_1.5CoFeMnO_9−δ (NBCFM) cathodes for IT-SOFC is investigated in this work. The interfacial polarization resistance (R_P) of NBCFM is 1.1273 Ω cm²~0.1587 Ω cm² in the range of 700–800 °C, showing good electrochemical performance. The linear thermal expansion coefficient of NBCFM is 17.40 × 10⁻⁶ K⁻¹ at 40–800 °C, which is significantly higher than that of the electrolyte. In order to further improve the electrochemical performance and reduce the thermal expansion coefficient (TEC) of NBCFM, Ce_0.8Sm_0.2O_2−δ (SDC) is mixed with NBCFM to prepare an NBCFM-xSDC composite cathode (x = 0, 10, 20, 30, 40 wt.%). The thermal expansion coefficient decreases monotonically from 17.40 × 10⁻⁶ K⁻¹ to 15.25 × 10⁻⁶ K⁻¹. The surface oxygen exchange coefficient of NBCFM-xSDC at a given temperature increases from 10⁻⁴ to 10⁻³ cm s⁻¹ over the po2 range from 0.01 to 0.09 atm, exhibiting fast surface exchange kinetics. The area specific resistance (ASR) of NBCFM-30%SDC is 0.06575 Ω cm² at 800 °C, which is only 41% of the ASR value of NBCFM (0.15872 Ω cm²). The outstanding performance indicates the feasibility of NBCFM-30% SDC as an IT-SOFC cathode material. This study provides a promising strategy for designing high-performance composite cathodes for SOFCs based on triple perovskite structures.     

Electrocatalytic Properties of Ni(II) Schiff Base Complex Polymer Films

Platinum electrodes were modified with polymers of the (±)-trans-N,N′-bis(salicylidene)-1,2-cyclohexanediaminenickel(II) ([Ni(salcn)]) and (±)-trans-N,N′-bis(3,3′-tert-Bu-salicylidene)-1,2-cyclohexanediaminenickel(II) ([Ni(salcn(Bu))]) complexes to study their electrocatalytic and electroanalytical properties. Poly[Ni(salcn)] and poly[Ni(salcn(Bu))]) modified electrodes catalyze the oxidation of catechol, aspartic acid and NO₂⁻. In the case of poly[Ni(salcn)] modified electrodes, the electrocatalysis process depends on the electroactive surface coverage. The films with low electroactive surface coverage are only a barrier in the path of the reducer to the electrode surface. The films with more electroactive surface coverage ensure both electrocatalysis inside the film and oxidation of the reducer directly on the electrode surface. In the films with the most electroactive surface coverage, electrocatalysis occurs only at the polymer–solution interface. The analysis was based on cyclic voltammetry, EQCM (electrochemical quartz crystal microbalance) and rotating disc electrode method.     

The Influence of Deposition Methods of Support Layer on Cordierite Substrate on the Characteristics of a MnO2–NiO–Co3O4/Ce0.2Zr0.8O2/Cordierite Three Way Catalyst

This paper compares different coating methods (in situ solid combustion, hybrid deposition, secondary growth on seed, suspension, double deposition of wet impregnation and suspension) to deposit Ce_0.2Zr_0.8O₂ mixed oxides on cordierite substrates, for use as a three way catalyst. Among them, the double deposition was proven to be the most efficient one. The coated sample shows a BET (Brunauer–Emmett–Teller) surface area of 25 m²/g, combined with a dense and crack free surface. The catalyst with a layer of MnO₂–NiO–Co₃O₄ mixed oxides on top of the Ce_0.2Zr_0.8O₂/cordierite substrate prepared by this method exhibits good activity for the treatment of CO, NO and C₃H₆ in exhaust gases (CO conversion of 100% at 250 °C, C₃H₆ conversion of 100% at 400 °C and NO conversion of 40% at 400 °C).     

Enhanced Structural Stability and Electrochemical Performance of LiNi0.6Co0.2Mn0.2O2 Cathode Materials by Ga Doping

Structural instability during cycling is an important factor affecting the electrochemical performance of nickel-rich ternary cathode materials for Li-ion batteries. In this work, enhanced structural stability and electrochemical performance of LiNi_0.6Co_0.2Mn_0.2O₂ cathode materials are achieved by Ga doping. Compared with the pristine electrode, Li[Ni_0.6Co_0.2Mn_0.2]_0.98Ga_0.02O₂ electrode exhibits remarkably improved electrochemical performance and thermal safety. At 0.5C rate, the discharge capacity increases from 169.3 mAh g⁻¹ to 177 mAh g⁻¹, and the capacity retention also rises from 82.8% to 89.8% after 50 cycles. In the charged state of 4.3 V, its exothermic temperature increases from 245.13 °C to more than 271.24 °C, and the total exothermic heat decreases from 561.7 to 225.6 J·g⁻¹. Both AC impedance spectroscopy and in situ XRD analysis confirmed that Ga doping can improve the stability of the electrode/electrolyte interface structure and bulk structure during cycling, which helps to improve the electrochemical performance of LiNi_0.6Co_0.2Mn_0.2O₂ cathode material.     

Annealing Effect on the Structural and Optical Properties of Sputter-Grown Bismuth Titanium Oxide Thin Films

The aim of this work is to assess the evolution of the structural and optical properties of Bi_xTi_yO_z films grown by rf magnetron sputtering upon post-deposition annealing treatments in order to obtain good quality films with large grain size, low defect density and high refractive index similar to that of single crystals. Films with thickness in the range of 220–250 nm have been successfully grown. After annealing treatment at 600 °C the films show excellent transparency and full crystallization. It is shown that to achieve larger crystallite sizes, up to 17 nm, it is better to carry the annealing under dry air than under oxygen atmosphere, probably because the nucleation rate is reduced. The refractive index of the films is similar under both atmospheres and it is very high (n =2.5 at 589 nm). However it is still slightly lower than that of the single crystal value due to the polycrystalline morphology of the thin films.